The Biology of the Prothoracicotropic Hormone Peptidergic Neurons in an Insect

SYNOPSIS. The prothoracicotropic hormone and the cerebral peptidergicneurons that produce it have traditionally been thought to havethe singular function of acting as a primary effector of insectpostembryonic development. Recent investigations of this neuroendocrineaxis in the tobacco hornworm, Manduca sexta, are leading toa new view that these peptidergic neurons and their peptidephenotypes may be multifunctional. They may act in differentways depending upon the animal's developmental stage and siteof phenotype release. The possibility for this functional diversityof the prothoracicotropic hormone is possibly even greater dueto multiple neuronal sites of peptide expression within thecentral nervous system. Similarly, the L-NSC III may have morefunctions due to the expression of multiple peptide phenotypes.The data, thus far, have not enabled us to identify additionalphysiological roles for the peptide, but they have providedinsight into the experimental approaches that might be effectivein resolving these functions.     

Endocrine Regulation of Lipid Synthesis in Decapod Crustaceans

The legulation of lipid synthesis in the hepatopancreas of thecrab Pachygrapsus crassipes and the crayfish Procambarus sp.was investigated. Although deatalking induces an increase inthe rate of ¹⁴C-1-acetate incorporation into lipid, injectionsof crustecdysone into intermolt animals fail to elicit a similarresponse. In addition, the increased rate of lipid synthesisinduced by destalking is unaffected by removal of the Y-organ.It would appear then that the increase in lipid synthesis characteristicof early premolt is not controlled by either crustecdysone orthe Y-organ. It is suggested that formation of acetyl-CoA byany one of a number of possible mechanisms may bethe mannerin which the increase in fatty acid synthesis is effected duringpremolt.     

The Prothoracicotropes: Source of the Prothoracicotropic Hormone

SYNOPSIS. An in vitro assay for the insect prothoracicolropichormone (PTTH) has been developed which measures the rate ofecdysone synthesized by Manduca sexta prothoracic glands (PG)stimulated in vitro by PTTH. This assay has been used to quantifyPTTH in single neurosecretory cells (NSC) resulting in the identificationof one NSC in each hemisphere of the brain as the prothoracicotrope,source of PTTH. The axonal and dendritic distribution of theprothoracicotrope has been determined by cobalt filling withsilver intensification. From a comparison of the titers of PTTHin brains, corpora cardiaca and corpora allata during larval-pupaldevelopment, the corpus allatum has been identifiedas the neurohemalorgan for PTTH. Electron microscopic analyses suggest that theacellular sheath surrounding the corpus allatum contains theaxon terminals of the prothoracicotropes. There is at least one form of PTTH, {small tilde}22,000 molwt (big PTTH), and possibly a smaller form of about 7,000 molwt (small PTTH). Bioassay and PTTH hemolymph titer data duringthe head critical period (HCP) for larval-larval developmentreveal that big PTTH is released as a single peak lasting {smalltilde}6 hr. By contrast, during the first HCP of the last larvalinstar PTTH is released over a period of {small tilde}18 hrin three bursts, but its molecular weight has not been establishedwith certainty. The kinetics of PG activation by these two formssuggest that big PTTH may function to activate the PG dramaticallyand thereby elicit molting, while small PTTH may activate thePG minimally at the time of cellular reprogramming.